The DOI matches its Crossref record; 61 of the 62 references it cites were found in a registry or an index.
Subpathways of nucleotide excision repair and their regulation
Abstract
Nucleotide excision repair provides an important cellular defense against a large variety of structurally unrelated DNA alterations. Most of these alterations, if unrepaired, may contribute to mutagenesis, oncogenesis, and developmental abnormalities, as well as cellular lethality. There are two subpathways of nucleotide excision repair; global genomic repair (GGR) and transcription coupled repair (TCR), that is selective for the transcribed DNA strand in expressed genes. Some of the proteins involved in the recognition of DNA damage (including RNA polymerase) are also responsive to natural variations in the secondary structural features of DNA. Gratuitous repair events in undamaged DNA might then contribute to genomic instability. However, damage recognition enzymes for GGR are normally maintained at very low levels unless the cells are genomically stressed. GGR is controlled through the SOS stress response in E. coli and through the activated p53 tumor suppressor in human cells. These inducible responses in human cells are important, as they have been shown to operate upon chemical carcinogen DNA damage at levels to which humans are environmentally exposed. Interestingly, most rodent tissues are deficient in the p53-dependent GGR pathway. Since rodents are used as surrogates for environmental cancer risk assessment, it is essential that we understand how they differ from humans with respect to DNA repair and oncogenic responses to environmental genotoxins. In the case of terminally differentiated mammalian cells, a new paradigm has appeared in which GGR is attenuated but both strands of expressed genes are repaired efficiently.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“One sub-pathway of NER, global genome NER (GG-NER), removes damage from the entire genome, whereas DNA damage in the transcribed strand of active genes is preferentially eliminated by transcription-coupled NER (TC-NER) [3].”
From NER initiation factors, DDB2 and XPC, regulate UV radiation response by recruiting ATR and ATM kinases to DNA damage sites (2013) · cites this paper as [3]
In the citing paper
“The NER pathway is subdivided into global genome repair (GG-NER) and transcription-coupled repair (TC-NER) [4].”
From Gap-filling and bypass at the replication fork are both active mechanisms for tolerance of low-dose ultraviolet-induced DNA damage in the human genome (2014) · cites this paper as [4]
Citations
Cites
Lindahl, T. L., & Wood, R. D. (1999) · Science · doi:10.1126/science.286.5446.1897 · Cited by 1,521
Bohr, V (1985) · Cell · doi:10.1016/0092-8674(85)90150-3 · Cited by 1,237 · cited 2×
“The analysis of the repair of UV-induced cyclobutane pyrimidine dimers (CPDs) in transcriptionally active versus inactive regions of the genome, and within transcribed and non-transcribed strands of expressed genes revealed the two distinct subpathways of nucleotide excision repair: TCR and GGR (Bohr et al., 1985; Mel…”
BackgroundMELLON, I. (1987) · Cell · doi:10.1016/0092-8674(87)90151-6 · Cited by 1,228
Sancar, A. (1996) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.65.070196.000355 · Cited by 1,131
Sugasawa, K., Ng, J. M. Y., Masutani, C., Iwai, S., van der Spek, P. J., Eker, A. P. M., Hanaoka, F., Bootsma, D., & Hoeijmakers, J. H. J. (1998) · Molecular Cell · doi:10.1016/s1097-2765(00)80132-x · Cited by 899
Courcelle, J., Khodursky, A., Peter, B., Brown, P. O., & Hanawalt, P. C. (2001) · Genetics · doi:10.1093/genetics/158.1.41 · Cited by 853
Self-citationMolecular Mechanisms for Repair of DNA
Hanawalt, P. C., & Setlow, R. B. (1975) · Springer eBooks · doi:10.1007/978-1-4684-2895-7 · Cited by 671
Self-citationMolecular Mechanism of Transcription-Repair Coupling
Selby, C. P., & Sancar, A. (1993) · Science · doi:10.1126/science.8465200 · Cited by 656
Hwang, B. J., Ford, J. M., Hanawalt, P. C., & Chu, G. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.2.424 · Cited by 581
Self-citationMellon, I., & Hanawalt, P. C. (1989) · Nature · doi:10.1038/342095a0 · Cited by 573
Self-citation
Flagged first, then by citations
1 of the 62 references couldn’t be matched to a known paper.
Research works printed but not linked: 3
- Ganesan AK, Spivak G, Hanawalt PC . 1983 Manipulation and Expression of Genes in Eukaryotes Nagley P, Linnane AW, Peacock WJ, Pateman JA (eds) Australia: Academic Press pp. 45–54
- Hanawalt PC, Bohr VA, Leadon SA, Mansbridge JN, Reush MKH . 1987 Processes in Cutaneous Epidermal Differentiation Bernstein I and Hirone T (eds) New York: Praeger Scientific pp. 217–231
- Nouspikel T, Hanawalt PC . 2003 Bioessays (in press)
Cited by
Sorted by citations
Items 201–300 of 442
Differential contribution of XPC, RAD23A, RAD23B and CENTRIN 2 to the UV-response in human cells
Renaud, E., Miccoli, L., Zacal, N., Biard, D. S. F., Craescu, C. T., Rainbow, A. J., & Angulo, J. F. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.05.003 · Cited by 31
Transcription factor IIS impacts UV-inhibited transcription
Jensen, A., & Mullenders, L. H. F. (2010) · DNA repair · doi:10.1016/j.dnarep.2010.08.002 · Cited by 28
The ERCC6 Gene and Age-Related Macular Degeneration
Baas, D. C., Despriet, D. D. G., Gorgels, T. G. M. F., Sawitzke, J., Uitterlinden, A. G., Albert Hofman, D., van Duijn, C. M., Merriam, J. E., Smith, R. T., Barile, G. R., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013786 · Cited by 28
Polymorphism of DNA repair genes in breast cancer
Smolarz, B., Michalska, M., Samulak, D., Romanowicz, H., & Wójcik, L. (2019) · Oncotarget · doi:10.18632/oncotarget.26568 · Cited by 28
Spontaneous mutagenesis associated with nucleotide excision repair in Escherichia coli
Hasegawa, K., Yoshiyama, K., & Maki, H. (2008) · Genes to Cells · doi:10.1111/j.1365-2443.2008.01185.x · Cited by 28
Smolarz, B., Makowska, M., Samulak, D., Michalska, M., Mojs, E. H., Wilczak, M., & Romanowicz, H. (2014) · Tumor Biology · doi:10.1007/s13277-013-1461-0 · Cited by 27
Mechanism of RNA polymerase II stalling by DNA alkylation
Malvezzi, S., Farnung, L., Aloisi, C. M. N., Angelov, T., Cramer, P., & Sturla, S. J. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1706592114 · Cited by 27
Singh, V., Azad, G. K., Mandal, P., Reddy, M., & Tomar, R. S. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.02.017 · Cited by 27
ERCC1: Impact in Multimodality Treatment of Upper Gastrointestinal Cancer
Metzger, R., Bollschweiler, E., Hölscher, A. H., & Warnecke‐Eberz, U. (2010) · Future Oncology · doi:10.2217/fon.10.140 · Cited by 28
Yeast Elc1 plays an important role in global genomic repair but not in transcription coupled repair
LeJeune, D., Chen, X., Ruggiero, C., Berryhill, S., Ding, B., & Li, S. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.08.010 · Cited by 27
Nucleotide excision repair in chromatin: The shape of things to come
Reed, S. H. (2005) · DNA repair · doi:10.1016/j.dnarep.2005.04.009 · Cited by 27
Lineage-specific control of TFIIH by MITF determines transcriptional homeostasis and DNA repair
Seoane, M., Buhs, S., Iglesias, P., Strauß, J., Puller, A., Müller, J., Gerull, H., Feldhaus, S., Alawi, M., Brandner, J. M., et al. (2019) · Oncogene · doi:10.1038/s41388-018-0661-x · Cited by 28
Navigating the nucleotide excision repair threshold
Liu, L., Lee, J., & Zhou, P. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22205 · Cited by 28
Cline, S. D., Lodeiro, M. F., Marnett, L. J., Cameron, C. E., & Arnold, J. J. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq656 · Cited by 26
Mutation and Recombination Rates Vary Across Bacterial Chromosome
Kivisaar, M. (2019) · Microorganisms · doi:10.3390/microorganisms8010025 · Cited by 26
Hsu, P.-H., Hanawalt, P. C., & Nouspikel, T. (2006) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2006.06.008 · Cited by 27
Self-citationZhou, T., Chen, P., Gu, J. H., Bishop, A. J. R., Scott, L., Hasty, P., & Rebel, V. I. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms16010966 · Cited by 26
Gossage, L., & Madhusudan, S. (2007) · Molecular Diagnosis & Therapy · doi:10.1007/bf03256260 · Cited by 26
Schreck, I., Chudziak, D., Schneider, S., Seidel, A., Platt, K. L., Oesch, F., & Weiß, C. (2009) · Toxicology · doi:10.1016/j.tox.2009.02.006 · Cited by 26
The Influence of Circadian Rhythms on DNA Damage Repair in Skin Photoaging
Su, Z. G., Hu, Q., Li, X., Wang, Z., & Xie, Y. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252010926 · Cited by 26
Lin, P. S., McPherson, L. A., Chen, A. Y., Sage, J., & Ford, J. M. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.03.003 · Cited by 27
Mitochondrial CSA and CSB: Protein interactions and protection from ageing associated DNA mutations
Kamenisch, Y., & Berneburg, M. (2013) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2013.03.005 · Cited by 25
ERCC4 variants identified in a cohort of patients with segmental progeroid syndromes
Mori, T., Yousefzadeh, M. J., Faridounnia, M., Chong, J. X., Hisama, F. M., Hudgins, L., Mercado, G., Wade, E. A., Barghouthy, A. S., Lee, L., et al. (2017) · Human Mutation · doi:10.1002/humu.23367 · Cited by 25
Lippert, M. J., Freedman, J. A., Barber, M. A., & Jinks-Robertson, S. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.11.4801-4809.2004 · Cited by 26
Role of Claspin in regulation of nucleotide excision repair factor DDB2
Prætorius-Ibba, M., Wang, Q.-E., Wani, G., El-Mahdy, M. A., Zhu, Q., Qin, S., & Wani, A. A. (2007) · DNA Repair · doi:10.1016/j.dnarep.2006.11.009 · Cited by 24
Ultraviolet-induced RNA:DNA hybrids interfere with chromosomal DNA synthesis
Kouzminova, E. A., & Kuzminov, A. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab147 · Cited by 24
Piao, M. J., Hewage, S. R. K. M., Han, X., Kang, K. A., Kang, H. K., Lee, N. H., & Hyun, J. W. (2015) · Marine Drugs · doi:10.3390/md13095629 · Cited by 24
DNA damage induced by the anthracycline cosmomycin D in DNA repair-deficient cells
Carvalho, H., Garrido, L. M., Furlan, R. L. A., Padilla, G., Agnoletto, M. H., Guecheva, T. N., Henriques, J. A. P., Saffi, J., & Menck, C. F. M. (2010) · Cancer Chemotherapy and Pharmacology · doi:10.1007/s00280-010-1244-x · Cited by 24
Bess, A. S., Leung, M. C. K., Ryde, I. T., Rooney, J. P., Hinton, D. E., & Meyer, J. N. (2013) · Worm · doi:10.4161/worm.23763 · Cited by 25
Aboussekhra, A., & Al-Sharif, I. S. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600665 · Cited by 24
Maddukuri, L., Dudzińska, D., & Tudek, B. (2007) · Acta Biochimica Polonica · doi:10.18388/abp.2007_3222 · Cited by 24
Multiple roles of ubiquitination in the control of nucleotide excision repair
Nouspikel, T. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.03.003 · Cited by 26
Regulation of various DNA repair pathways by E3 ubiquitin ligases
Natarajan, C., & Takeda, K. (2017) · Journal of Cancer Research and Therapeutics · doi:10.4103/0973-1482.204879 · Cited by 25
Rivera-Begeman, A., McDaniel, L. D., Schultz, R. A., & Friedberg, E. C. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.09.008 · Cited by 23
Solovjeva, L., Svetlova, M., Sasina, L., Tanaka, K., Saijo, M., Nazarov, I. B., Bradbury, M., & Tomilin, N. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-12-1066 · Cited by 23
Chen, C.-Y., Kawasumi, M., Lan, T.-Y., Poon, C.-L., Lin, Y.-S., Wu, P.-J., Chen, Y.-C., Chen, B., Wu, C., Lo, J., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010355 · Cited by 22
Hyka‐Nouspikel, N., Lemonidis, K., Lu, W.-T., & Nouspikel, T. (2011) · Blood · doi:10.1182/blood-2010-12-326637 · Cited by 23
Mitochondrial DNA Damage Does Not Determine C. elegans Lifespan
Ng, L. F., Ng, L. T., van Breugel, M., Halliwell, B. B., & Gruber, J. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00311 · Cited by 22
Zhang, L., Jones, K. L., & Gong, F. (2009) · Biochemistry and Cell Biology · doi:10.1139/o08-101 · Cited by 22
STI571 reduces NER activity in BCR/ABL-expressing cells
Śliwiński, T., Czechowska, A., Szemraj, J., Morawiec, Z., Skórski, T., & Błasiak, J. (2008) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2008.06.002 · Cited by 22
Mirzayans, R., Scott, A., Andrais, B., Pollock, S., & Murray, D. L. (2007) · Journal of Cellular Physiology · doi:10.1002/jcp.21284 · Cited by 23
Romano, V., Napoli, A., Salerno, V., Valenti, A., Rossi, M., & Ciaramella, M. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.10.045 · Cited by 22
Protein degradation in DNA damage response
Kouranti, I., & Peyroche, A. (2012) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2012.02.004 · Cited by 26
Diderich, K. E. M., Nicolaije, C., Priemel, M., Waarsing, J. H., Day, J. S., Brandt, R. M. C., Schilling, A. F., Botter, S. M., Weinans, H., van der Horst, G. T. J., et al. (2011) · AGE · doi:10.1007/s11357-011-9291-8 · Cited by 22
Stereoselective excision of thymine glycol lesions by mammalian cell extracts
McTigue, M. M., Rieger, R. A., Rosenquist, T. A., Iden, C. R., & Santos, C. R. D. L. (2003) · DNA repair · doi:10.1016/j.dnarep.2003.11.009 · Cited by 22
DNA repair mechanisms and Toxoplasma gondii infection
Smolarz, B., Wilczyński, J., & Nowakowska, D. (2013) · Archives of Microbiology · doi:10.1007/s00203-013-0944-0 · Cited by 21
Slyšková, J., Cordero, F., Pardini, B., Korenková, V., Vymetalkova, V. P., Bielik, L., Vodičková, Ľ., Pitule, P., Liška, V., Matějka, V. M., et al. (2014) · Molecular Carcinogenesis · doi:10.1002/mc.22141 · Cited by 21
Ho, H. N., van Oijen, A. M., & Ghodke, H. B. (2020) · Nature Communications · doi:10.1038/s41467-020-15182-3 · Cited by 21
p53: Guardian of a Genome's Guardian?
Rubbi, C. P., & Milner, J. (2003) · Cell Cycle · doi:10.4161/cc.2.1.297 · Cited by 21
Piao, M. J., Ahn, M. J., Kang, K. A., Kim, K. C., Cha, J. W., Lee, N. H., & Hyun, J. W. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.02.019 · Cited by 21
Gutierrez-Mariscal, F. M., Yubero‐Serrano, E. M., Rangel-Zúñiga, O. A., Marı́n, C., García‐Ríos, A., Pérez‐Martínez, P., Delgado‐Lista, J., Malagón, M. M., Tinahones, F. J., Pérez‐Jiménez, F., et al. (2013) · The Journals of Gerontology Series A · doi:10.1093/gerona/glt174 · Cited by 21
Miccoli, L., Burr, K., Hickenbotham, P. T., Friedberg, E. C., Angulo, J. F., & Dubrova, Y. E. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-3844 · Cited by 24
Molecular Interactions between Dietary Lipids and Bone Tissue during Aging
Romero‐Márquez, J. M., Varela‐López, A., Navarro‐Hortal, M. D., Badillo-Carrasco, A., Forbes-Hernández, T. Y., Giampieri, F., Azpíroz, I. D., Madrigal, L., Battino, M. A., & Quiles, J. L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126473 · Cited by 20
Wu, H., Li, S., Hu, X., Qin, W., Wang, Y., Sun, T., Wu, Z., Wang, X., Lu, S., Xu, D.-P., et al. (2019) · Journal of Cancer · doi:10.7150/jca.30975 · Cited by 20
Moser, B., Basílio, J., Gotzmann, J., Brachner, A., & Foisner, R. (2020) · Cells · doi:10.3390/cells9020463 · Cited by 20
The contribution of mitochondrial thymidylate synthesis in preventing the nuclear genome stress
Lee, M.-H., Wang, L., & Chang, Z.-F. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku152 · Cited by 20
DNA damage response and neuroprotection
Kruman, I. I. (2007) · Frontiers in bioscience · doi:10.2741/2862 · Cited by 20
Brown, P. J., Bedard, L. L., & Massey, T. E. (2007) · Cancer Letters · doi:10.1016/j.canlet.2007.10.015 · Cited by 20
UV-inducible base excision repair of oxidative damaged DNA in human cells
Kassam, S. N., & Rainbow, A. J. (2008) · Mutagenesis · doi:10.1093/mutage/gen054 · Cited by 19
hnRNP A1 promotes keratinocyte cell survival post UVB radiation through PI3K/Akt/mTOR pathway
Feng, J., Liao, Y., Xu, X., Yi, Q., He, L., & Tang, L. (2017) · Experimental Cell Research · doi:10.1016/j.yexcr.2017.12.002 · Cited by 19
Two Sides of the Same Coin: TFIIH Complexes in Transcription and DNA Repair
Zhovmer, A. S., Oksenych, V., & Coin, F. (2010) · The Scientific World JOURNAL · doi:10.1100/tsw.2010.46 · Cited by 21
Mouchet, N., Adamski, H., Bouvet, R., Corre, S., Courbebaisse, Y., Watier, É., Mosser, J., Chesné, C., & Galibert, M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010776 · Cited by 20
Nicolaije, C., Diderich, K. E. M., Botter, S. M., Priemel, M., Waarsing, J. H., Day, J. S., Brandt, R. M. C., Schilling, A. F., Weinans, H., van der Eerden, B. C. J., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035246 · Cited by 18
The HTLV-I Tax oncoprotein: hyper-tasking at the molecular level
Diane, R. W. (2005) · Frontiers in bioscience · doi:10.2741/1558 · Cited by 18
Non-transcribed strand repair revealed in quiescent cells
Bielas, J. H. (2006) · Mutagenesis · doi:10.1093/mutage/gei073 · Cited by 18
Strippoli, A., Rossi, S., Martini, M., Basso, M., D’Argento, E., Schinzari, G., Barile, R., Cassano, A., & Barone, C. A. (2016) · Oncotarget · doi:10.18632/oncotarget.9063 · Cited by 17
c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum
Senhaji, M. A., Abidi, O., Nadifi, S., Benchikhi, H., Khadir, K., Rekaya, M. B., Eloualid, A., Messaoud, O., Abdelhak, S., & Barakat, A. (2012) · Archives of Dermatological Research · doi:10.1007/s00403-012-1299-0 · Cited by 17
Overview of DNA repair pathways, current targets, and clinical trials bench to clinic
Kelley, M. R., & Fishel, M. L. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803582-5.00001-2 · Cited by 18
A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome
Taghdiri, M., Dastsooz, H., Fardaei, M., Mohammadi, S., Fard, M. A. F., & Faghihi, M. A. (2017) · Frontiers in Pediatrics · doi:10.3389/fped.2017.00169 · Cited by 16
Smolarz, B., Michalska, M., Samulak, D., Wójcik, L., & Romanowicz, H. (2018) · Anticancer Research · doi:10.21873/anticanres.12846 · Cited by 16
Carvalho, H., Ortolan, T. G., dePaula, T., Leite, R. A., Weinlich, R., Amarante-Mendes, G. P., & Menck, C. F. M. (2008) · DNA repair · doi:10.1016/j.dnarep.2008.03.003 · Cited by 16
Alice, A. F., Cristovao, F., & Pereira-Wilso, C. (2011) · InTech eBooks · doi:10.5772/22125 · Cited by 17
Slowly Progressing Nucleotide Excision Repair in Trichothiodystrophy Group A Patient Fibroblasts
Theil, A. F., Nonnekens, J., Wijgers, N., Vermeulen, W., & Giglia‐Mari, G. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.01462-10 · Cited by 15
Takahashi, A., Shibata, N., Nishikawa, S., Ohnishi, K., Ishioka, N., & Ohnishi, T. (2006) · Photochemical & Photobiological Sciences · doi:10.1039/b601971d · Cited by 15
Mutagenesis and the three R's in yeast
Abdulovic, A. L., Kim, N., & Jinks-Robertson, S. (2006) · DNA repair · doi:10.1016/j.dnarep.2005.11.006 · Cited by 15
Nikiforov, A. A., Svetlova, M., Solovjeva, L., Sasina, L., Siino, J. S., Nazarov, I. B., Bradbury, M., & Tomilin, N. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.08.165 · Cited by 15
Genotoxic Stress, DNA Repair, and Crop Productivity
Balestrazzi, A., Macovei, A., Donà, M., Carbonera, D., & Confalonieri, M. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4633-0_7 · Cited by 15
An Experimental Model for Assessment of Global DNA Repair Capacity
Chakarov, S., Roeva, I., & Russev, G. C. (2011) · Biotechnology & Biotechnological Equipment · doi:10.5504/bbeq.2011.0080 · Cited by 14
Michalska, M., Samulak, D., Romanowicz, H., Sobkowski, M., & Smolarz, B. (2015) · Advances in Medicine · doi:10.1155/2015/109593 · Cited by 14
CometChip enables parallel analysis of multiple DNA repair activities
Ge, J., Ngo, L. P., Kaushal, S., Tay, I. J. J., Thadhani, E., Kay, J. E., Mazzucato, P., Chow, D. N., Fessler, J. L., Weingeist, D. M., et al. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103176 · Cited by 14
Detection of bulky DNA lesions: DDB2 at the interface of chromatin and DNA repair in eukaryotes
Jones, K. L., Zhang, L., Seldeen, K. L., & Gong, F. (2010) · IUBMB Life · doi:10.1002/iub.391 · Cited by 14
Regulation of nucleotide excision repair through ubiquitination
Li, J., Bhat, A., & Xiao, W. (2011) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmr088 · Cited by 16
Das, D., Faridounnia, M., Kovačič, L., Kaptein, R., Boelens, R., & Folkers, G. E. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.747857 · Cited by 16
Is the repair of oxidative DNA base modifications inducible by a preceding DNA damage induction?
Bercht, M., Flohr-Beckhaus, C., Osterod, M., Rünger, T. M., Radicella, J. P., & Epe, B. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.11.007 · Cited by 14
SUMOylation of damaged DNA-binding protein DDB2
Tsuge, M., Masuda, Y., Kaneoka, H., Kidani, S., Miyake, K., & Iijima, S. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.07.013 · Cited by 14
DNA Damage Response Pathways and Cancer
Ford, J. M., & Kastan, M. B. (2014) · Elsevier eBooks · doi:10.1016/b978-1-4557-2865-7.00010-2 · Cited by 14
DNA Repair and Cell Differentiation—Does Getting Older Means Getting Wiser as Well?
Chakarov, S., & Russev, G. (2010) · Biotechnology & Biotechnological Equipment · doi:10.2478/v10133-010-0039-x · Cited by 13
Wieser, T. A., & Wuttke, D. (2022) · Biochemistry · doi:10.1021/acs.biochem.2c00504 · Cited by 14
DNA repair mechanisms and human cytomegalovirus (HCMV) infection
Smolarz, B., Wilczyński, J., & Nowakowska, D. (2014) · Folia Microbiologica · doi:10.1007/s12223-014-0359-6 · Cited by 13
Cell Cycle Arrest Induced by Radiation in Cultured Silkworm Cells
Takahashi, M., Lee, J. M., Mon, H., Kawaguchi, Y., Koga, K., & Kusakabe, T. (2006) · Journal of insect biotechnology and sericology · doi:10.11416/jibs.75.23 · Cited by 13
Testing excision models for responses of mismatch‐repair systems to UV photoproducts in DNA
Wang, H., Hoffman, P. D., Lawrence, C. W., & Hays, J. B. (2006) · Environmental and Molecular Mutagenesis · doi:10.1002/em.20206 · Cited by 13
Nucleotide excision repair deficiencies and the somatotropic axis in aging
Garinis, G. A. (2008) · HORMONES · doi:10.14310/horm.2002.1111032 · Cited by 13
Dregoesc, D., Rybak, A. P., & Rainbow, A. J. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.11.008 · Cited by 13
Structural Aspects of Polycyclic Aromatic Carcinogen-Damaged DNA and Its Recognition by NER Proteins
Patel, D. J., Naegeli, H., Broyde, S. B., & Geacintov, N. E. (2005) · CRC Press eBooks · doi:10.1201/9780849352683.ch13 · Cited by 13
Xeroderma Pigmentosum, Cockayne Syndrome and Trichothiodystrophy
Emmert, S. (2011) · Wiley eBooks · doi:10.1002/9781444345384.ch135 · Cited by 13
Leite, R. A. (2008) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2008.tde-27112008-165017 · Cited by 13
Lomonaco, S. L., Xu, X., & Wang, G. (2009) · DNA and Cell Biology · doi:10.1089/dna.2008.0815 · Cited by 13
Nucleotide Excision Repair from Bacteria to Humans: Structure–Function Studies
Ye, P., Wang, H., Santana‐Santos, L., Kisker, C., & Houten, B. V. (2010) · Humana Press eBooks · doi:10.1007/978-1-61737-995-6_13 · Cited by 12
Xu, X., Nakazawa, N., & Yanagida, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119347 · Cited by 12
Zhu, Q., Wani, G., Sharma, N., & Wani, A. A. (2012) · DNA repair · doi:10.1016/j.dnarep.2012.09.003 · Cited by 12
Metadata
- Authors
- Hanawalt, P. C.
- Affiliations
- Stanford University (US)
- Corresponding author
- Hanawalt, Philip C
- ORCID
- Hanawalt, Philip C
- Venue
- Oncogene
- Published
- 2002-12-16
- Volume
- 21
- Issue
- 58
- Pages
- 8949-8956
- ISSN
- 0950-9232 (ISSN-L)
- 1476-5594
- OpenAlex
- W1979123830
- Cited by
- 447
- References
- 62
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 7 · 2023: 4 · 2022: 6 · 2021: 12 · 2020: 11 · 2019: 11 · 2018: 9 · 2017: 11 · 2016: 14 · 2015: 20 · 2014: 20 · 2013: 24 · 2012: 24
- FWCI
- 1.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Oncogene (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (CA91456, R01CA077712, CA90915, R01CA090915, CA-44349, R35CA044349, CA-77712, R01CA091456)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Carcinogens and Genotoxicity Assessment
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Keywords
- nucleotide excision repair, transcription-coupled repair, DNA damage recognition, RNA polymerase, genomic instability, SOS response, p53, cancer risk assessment, terminally differentiated cells, mutagenesis
- MeSH terms
- Animals, Cell Differentiation, DNA Damage, DNA Repair, Escherichia coli, Humans, Neurons, Oncogenic Viruses, Species Specificity, Gene Expression Regulation, Bacterial, Tumor Suppressor Protein p53
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review